Reactions and Rearrangements in 2-Oxabicycloheptanones

DOI: 10.1021/jo00045a020

Source and publish data:

Journal of Organic Chemistry p. 5102 - 5105 (1992)

Update date:2022-08-04

Topics:

Authors:

Naidorf-Meir, Simha

Hassner, Alfred

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Article abstract of DOI:10.1021/jo00045a020

The furan-fused chlorocyclobutanone 6 undergoes reaction with O, N, S, C nucleophiles at a much slower rate than its pyran homolog, wich is attributed to a reluctance to enolization.Instead of substitution products, rearranged products were formed.For ins

Full text of DOI:10.1021/jo00045a020

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